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  • Barosi, G (author)

Clinical end points for drug treatment trials in BCR-ABL1-negative classic myeloproliferative neoplasms : consensus statements from European LeukemiaNET (ELN) and Internation Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT)

  • Article/chapterEnglish2015

Publisher, publication year, extent ...

  • 2014-08-25
  • Springer Science and Business Media LLC,2015
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-239848
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-239848URI
  • https://doi.org/10.1038/leu.2014.250DOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:130480588URI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • The discovery of somatic mutations, primarily JAK2V617F and CALR, in classic BCR-ABL1-negative myeloproliferative neoplasms (MPNs) has generated interest in the development of molecularly targeted therapies, whose accurate assessment requires a standardized framework. A working group, comprised of members from European LeukemiaNet (ELN) and International Working Group for MPN Research and Treatment (IWG-MRT), prepared consensus-based recommendations regarding trial design, patient selection and definition of relevant end points. Accordingly, a response able to capture the long-term effect of the drug should be selected as the end point of phase II trials aimed at developing new drugs for MPNs. A time-to-event, such as overall survival, or progression-free survival or both, as co-primary end points, should measure efficacy in phase III studies. New drugs should be tested for preventing disease progression in myelofibrosis patients with early disease in randomized studies, and a time to event, such as progression-free or event-free survival should be the primary end point. Phase III trials aimed at preventing vascular events in polycythemia vera and essential thrombocythemia should be based on a selection of the target population based on new prognostic factors, including JAK2 mutation. In conclusion, we recommended a format for clinical trials in MPNs that facilitates communication between academic investigators, regulatory agencies and drug companies.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Tefferi, A (author)
  • Besses, C (author)
  • Birgegård, GunnarUppsala universitet,Hematologi(Swepub:uu)gunnarbg (author)
  • Cervantes, F (author)
  • Finazzi, G (author)
  • Gisslinger, H (author)
  • Griesshammer, M (author)
  • Harrison, C (author)
  • Hehlmann, R (author)
  • Hermouet, S (author)
  • Kiladjian, J-J (author)
  • Kröger, N (author)
  • Mesa, R (author)
  • Mc Mullin, M F (author)
  • Pardanani, A (author)
  • Passamonti, F (author)
  • Samuelsson, JKarolinska Institutet (author)
  • Vannucchi, A M (author)
  • Reiter, A (author)
  • Silver, R T (author)
  • Verstovsek, S (author)
  • Tognoni, G (author)
  • Barbui, T (author)
  • Uppsala universitetHematologi (creator_code:org_t)

Related titles

  • In:Leukemia: Springer Science and Business Media LLC29:1, s. 20-260887-69241476-5551

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